Drug recall
Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
FDA recall event 98871 · Class II · Covidien, LP
Key facts
| Event ID | 98871 |
|---|---|
| Recall numbers | Z-2281-2026 |
| Recalling firm | Covidien, LP |
| Product type | Devices |
| Products | Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure. |
| Initiation date | Apr 15, 2026 |
| Report date | Jun 10, 2026 |
| City | North Haven |
| State | CT |
| Country | United States |
| FEI number | 1219930 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: